Please use this identifier to cite or link to this item:
https://ahro.austin.org.au/austinjspui/handle/1/16726
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DC Field | Value | Language |
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dc.contributor.author | Hertzberg, Mark | - |
dc.contributor.author | Gandhi, Maher K | - |
dc.contributor.author | Trotman, Judith | - |
dc.contributor.author | Butcher, Belinda | - |
dc.contributor.author | Taper, John | - |
dc.contributor.author | Johnston, Amanda | - |
dc.contributor.author | Gill, Devinder | - |
dc.contributor.author | Ho, Shir-Jing | - |
dc.contributor.author | Cull, Gavin | - |
dc.contributor.author | Fay, Keith | - |
dc.contributor.author | Chong, Geoffrey | - |
dc.contributor.author | Grigg, Andrew P | - |
dc.contributor.author | Lewis, Ian D. | - |
dc.contributor.author | Milliken, Sam | - |
dc.contributor.author | Renwick, William | - |
dc.contributor.author | Hahn, Uwe | - |
dc.contributor.author | Filshie, Robin | - |
dc.contributor.author | Kannourakis, George | - |
dc.contributor.author | Watson, Anne-Marie | - |
dc.contributor.author | Warburton, Pauline | - |
dc.contributor.author | Wirth, Andrew | - |
dc.contributor.author | Seymour, John F | - |
dc.contributor.author | Hofman, Michael S | - |
dc.contributor.author | Hicks, Rodney J | - |
dc.contributor.author | Australasian Leukaemia and Lymphoma Group (ALLG) | - |
dc.date | 2016-11-10 | - |
dc.date.accessioned | 2017-07-26T00:50:44Z | - |
dc.date.available | 2017-07-26T00:50:44Z | - |
dc.date.issued | 2017-02 | - |
dc.identifier.citation | Haematologica 2017; 102(2): 356-363 | en_US |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/16726 | - |
dc.description.abstract | In the treatment of diffuse large B-cell lymphoma, a persistently positive [18F]fluorodeoxyglucose positron emission tomography (PET) scan typically carries a poor prognosis. In this prospective multi-center phase II study, we sought to establish whether treatment intensification with R-ICE (rituximab, ifosfamide, carboplatin, and etoposide) chemotherapy followed by 90Y-ibritumomab tiuxetan-BEAM (BCNU, etoposide, cytarabine, and melphalan) for high-risk diffuse large B-cell lymphoma patients who are positive on interim PET scan after 4 cycles of R-CHOP-14 (rituximab, cyclophosphamide, doxorubicin, and prednisone) can improve 2-year progression-free survival from a historically unfavorable rate of 40% to a rate of 65%. Patients received 4 cycles of R-CHOP-14, followed by a centrally-reviewed PET performed at day 17-20 of cycle 4 and assessed according to International Harmonisation Project criteria. Median age of the 151 evaluable patients was 57 years, with 79% stages 3-4, 54% bulk, and 54% International Prognostic Index 3-5. Among the 143 patients undergoing interim PET, 101 (71%) were PET-negative (96 of whom completed R-CHOP), 42 (29%) were PET-positive (32 of whom completed R-ICE and 90Y-ibritumomab tiuxetan-BEAM). At a median follow up of 35 months, the 2-year progression-free survival for PET-positive patients was 67%, a rate similar to that for PET-negative patients treated with R-CHOP-14 (74%, P=0.11); overall survival was 78% and 88% (P=0.11), respectively. In an exploratory analysis, progression-free and overall survival were markedly superior for PET-positive Deauville score 4 versus score 5 (P=0.0002 and P=0.001, respectively). Therefore, diffuse large B-cell lymphoma patients who are PET-positive after 4 cycles of R-CHOP-14 and who switched to R-ICE and 90Y-ibritumomab tiuxetan-BEAM achieved favorable survival outcomes similar to those for PET-negative R-CHOP-14-treated patients. Further studies are warranted to confirm these promising results. (Registered at: ACTRN12609001077257). | en_US |
dc.subject | Antineoplastic Combined Chemotherapy Protocols | en_US |
dc.subject | Lymphoma, Large B-Cell, Diffuse | en_US |
dc.subject | Positron-Emission Tomography | en_US |
dc.title | Early treatment intensification with R-ICE and 90Y-ibritumomab tiuxetan (Zevalin)-BEAM stem cell transplantation in patients with high-risk diffuse large B-cell lymphoma patients and positive interim PET after 4 cycles of R-CHOP-14 | en_US |
dc.type | Journal Article | en_US |
dc.identifier.journaltitle | Haematologica | en_US |
dc.identifier.affiliation | Department of Haematology, Prince of Wales Hospital and University of NSW, Randwick, NSW, Australia | en_US |
dc.identifier.affiliation | The University of Queensland Diamantina Institute Woolloongabba, Brisbane, QLD, Australia | en_US |
dc.identifier.affiliation | Department of Haematology, Princess Alexandra Hospital, Brisbane, QLD, Australia | en_US |
dc.identifier.affiliation | Department of Haematology, Repatriation General Hospital Concord and University of Sydney, NSW, Australia | en_US |
dc.identifier.affiliation | WriteSource Medical Pty Ltd., Lane Cove, NSW, Australia | en_US |
dc.identifier.affiliation | Nepean Cancer Care Centre, Nepean Hospital, Nepean, NSW, Australia | en_US |
dc.identifier.affiliation | Department of Haematology, Westmead Hospital, NSW, Australia | en_US |
dc.identifier.affiliation | Department of Haematology, St George Hospital, Kogarah, NSW, Australia | en_US |
dc.identifier.affiliation | Department of Haematology, Sir Charles Gairdner Hospital, Perth, WA, Australia | en_US |
dc.identifier.affiliation | Department of Haematology, Royal North Shore Hospital, St Leonard's, NSW, Australia | en_US |
dc.identifier.affiliation | Olivia Newton John Cancer & Wellness Centre, Austin Health, Heidelberg, Victoria, Australia | en_US |
dc.identifier.affiliation | Department of Haematology, Austin Health, Heidelberg, Victoria, Australia | en_US |
dc.identifier.affiliation | Department of Haematology, Royal Adelaide Hospital, Adelaide, SA, Australia | en_US |
dc.identifier.affiliation | Department of Haematology, St Vincent's Hospital Darlinghurst, NSW, Australia | en_US |
dc.identifier.affiliation | Department of Haematology, Royal Melbourne Hospital, Parkville, Victoria, Australia | en_US |
dc.identifier.affiliation | Department of Haematology, The Queen Elizabeth Hospital, SA, Australia | en_US |
dc.identifier.affiliation | Department of Haematology, St Vincent's Hospital, Melbourne, Victoria, Australia | en_US |
dc.identifier.affiliation | Ballarat Oncology and Haematology Service and Fiona Elsey Cancer Research Institute, Ballarat, Victoria, Australia | en_US |
dc.identifier.affiliation | Department of Haematology, Liverpool Hospital, Liverpool, NSW, Australia | en_US |
dc.identifier.affiliation | Department of Haematology, Wollongong Hospital, Wollongong, NSW, Australia | en_US |
dc.identifier.affiliation | Department of Radiation Oncology, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia | en_US |
dc.identifier.affiliation | Department of Haematology, Peter MacCallum Cancer Centre East Melbourne and University of Melbourne, Parkville, Victoria, Australia | en_US |
dc.identifier.affiliation | Department of Cancer Imaging, Peter MacCallum Cancer Centre East Melbourne, Victoria, Australia | en_US |
dc.identifier.pubmeduri | https://pubmed.ncbi.nlm.nih.gov/28143954 | en_US |
dc.identifier.doi | 10.3324/haematol.2016.154039 | en_US |
dc.type.content | Text | en_US |
dc.type.austin | Journal Article | en_US |
local.name.researcher | Chong, Geoffrey | |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
item.openairetype | Journal Article | - |
crisitem.author.dept | Olivia Newton-John Cancer Wellness and Research Centre | - |
crisitem.author.dept | Olivia Newton-John Cancer Wellness and Research Centre | - |
crisitem.author.dept | Clinical Haematology | - |
Appears in Collections: | Journal articles |
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